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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 11-65541130-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=65541130&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 65541130,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "ENST00000301873.11",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2889C>T",
"hgvs_p": "p.Ser963Ser",
"transcript": "NM_001130144.3",
"protein_id": "NP_001123616.1",
"transcript_support_level": null,
"aa_start": 963,
"aa_end": null,
"aa_length": 1303,
"cds_start": 2889,
"cds_end": null,
"cds_length": 3912,
"cdna_start": 3289,
"cdna_end": null,
"cdna_length": 4833,
"mane_select": "ENST00000301873.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2889C>T",
"hgvs_p": "p.Ser963Ser",
"transcript": "ENST00000301873.11",
"protein_id": "ENSP00000301873.5",
"transcript_support_level": 2,
"aa_start": 963,
"aa_end": null,
"aa_length": 1303,
"cds_start": 2889,
"cds_end": null,
"cds_length": 3912,
"cdna_start": 3289,
"cdna_end": null,
"cdna_length": 4833,
"mane_select": "NM_001130144.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2889C>T",
"hgvs_p": "p.Ser963Ser",
"transcript": "ENST00000322147.8",
"protein_id": "ENSP00000326647.4",
"transcript_support_level": 1,
"aa_start": 963,
"aa_end": null,
"aa_length": 1256,
"cds_start": 2889,
"cds_end": null,
"cds_length": 3771,
"cdna_start": 2889,
"cdna_end": null,
"cdna_length": 4046,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2534C>T",
"hgvs_p": null,
"transcript": "ENST00000528516.5",
"protein_id": "ENSP00000432350.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3935,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2534C>T",
"hgvs_p": null,
"transcript": "ENST00000528516.5",
"protein_id": "ENSP00000432350.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3935,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2766C>T",
"hgvs_p": "p.Ser922Ser",
"transcript": "ENST00000689505.1",
"protein_id": "ENSP00000510401.1",
"transcript_support_level": null,
"aa_start": 922,
"aa_end": null,
"aa_length": 1262,
"cds_start": 2766,
"cds_end": null,
"cds_length": 3789,
"cdna_start": 3166,
"cdna_end": null,
"cdna_length": 4710,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2889C>T",
"hgvs_p": "p.Ser963Ser",
"transcript": "NM_021070.4",
"protein_id": "NP_066548.2",
"transcript_support_level": null,
"aa_start": 963,
"aa_end": null,
"aa_length": 1256,
"cds_start": 2889,
"cds_end": null,
"cds_length": 3771,
"cdna_start": 3158,
"cdna_end": null,
"cdna_length": 4561,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2622C>T",
"hgvs_p": "p.Ser874Ser",
"transcript": "ENST00000530866.6",
"protein_id": "ENSP00000435276.2",
"transcript_support_level": 2,
"aa_start": 874,
"aa_end": null,
"aa_length": 1214,
"cds_start": 2622,
"cds_end": null,
"cds_length": 3645,
"cdna_start": 2968,
"cdna_end": null,
"cdna_length": 4512,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2538C>T",
"hgvs_p": "p.Ser846Ser",
"transcript": "NM_001164266.1",
"protein_id": "NP_001157738.1",
"transcript_support_level": null,
"aa_start": 846,
"aa_end": null,
"aa_length": 1139,
"cds_start": 2538,
"cds_end": null,
"cds_length": 3420,
"cdna_start": 3154,
"cdna_end": null,
"cdna_length": 4557,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "c.2034C>T",
"hgvs_p": "p.Ser678Ser",
"transcript": "ENST00000526927.6",
"protein_id": "ENSP00000431219.2",
"transcript_support_level": 2,
"aa_start": 678,
"aa_end": null,
"aa_length": 971,
"cds_start": 2034,
"cds_end": null,
"cds_length": 2916,
"cdna_start": 2434,
"cdna_end": null,
"cdna_length": 3344,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.185C>T",
"hgvs_p": null,
"transcript": "ENST00000526124.1",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 347,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2152C>T",
"hgvs_p": null,
"transcript": "ENST00000526825.6",
"protein_id": "ENSP00000435146.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4498,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.854C>T",
"hgvs_p": null,
"transcript": "ENST00000529189.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1997,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.931C>T",
"hgvs_p": null,
"transcript": "ENST00000529582.6",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2464,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.1177C>T",
"hgvs_p": null,
"transcript": "ENST00000530785.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2461,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.396C>T",
"hgvs_p": null,
"transcript": "ENST00000530990.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 531,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.2043C>T",
"hgvs_p": null,
"transcript": "ENST00000532932.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3327,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.2561C>T",
"hgvs_p": null,
"transcript": "ENST00000685178.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3620,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.1390C>T",
"hgvs_p": null,
"transcript": "ENST00000688764.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2782,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"hgvs_c": "n.*2152C>T",
"hgvs_p": null,
"transcript": "ENST00000526825.6",
"protein_id": "ENSP00000435146.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4498,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "LTBP3",
"gene_hgnc_id": 6716,
"dbsnp": "rs75311576",
"frequency_reference_population": 0.0003930803,
"hom_count_reference_population": 2,
"allele_count_reference_population": 634,
"gnomad_exomes_af": 0.000210872,
"gnomad_genomes_af": 0.00214051,
"gnomad_exomes_ac": 308,
"gnomad_genomes_ac": 326,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.24699999392032623,
"computational_prediction_selected": "Benign",
"computational_source_selected": "REVEL",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.247,
"revel_prediction": "Benign",
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.52,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.066,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -14,
"acmg_classification": "Benign",
"acmg_criteria": "BP4,BP6_Very_Strong,BP7,BS1",
"acmg_by_gene": [
{
"score": -14,
"benign_score": 14,
"pathogenic_score": 0,
"criteria": [
"BP4",
"BP6_Very_Strong",
"BP7",
"BS1"
],
"verdict": "Benign",
"transcript": "ENST00000301873.11",
"gene_symbol": "LTBP3",
"hgnc_id": 6716,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.2889C>T",
"hgvs_p": "p.Ser963Ser"
}
],
"clinvar_disease": "Brachyolmia-amelogenesis imperfecta syndrome,Inborn genetic diseases,LTBP3-related disorder",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:1 B:1",
"phenotype_combined": "Brachyolmia-amelogenesis imperfecta syndrome|Inborn genetic diseases|LTBP3-related disorder",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}